未分化结缔组织病
医学
结缔组织
系统性红斑狼疮
疾病
结缔组织病
结缔组织病
病理
皮肤病科
自身免疫性疾病
作者
E Pestelli,Walter Volpi,Barbara Giomi,Marzia Caproni,Paolo Fabbri
标识
DOI:10.1046/j.1468-3083.2003.00822.x
摘要
Undifferentiated connective tissue disease (UCTD, also named UCT syndrome, latent lupus or incomplete lupus) is regarded as an autoimmune disorder in which signs and symptoms are widely variable and evocative for connectivitis but not sufficiently evolved to fulfil any of the accepted classification criteria for the defined connective tissue diseases. In this paper we describe the case of a 47-year-old woman affected by UCTD according to the preliminary classification criteria supplied by Mosca et al. in 1999.
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